Rosiglitazone and Cognitive Stability in Older Individuals With Type 2 Diabetes and Mild Cognitive Impairment

被引:76
|
作者
Abbatecola, Angela M. [2 ]
Lattanzio, Fabrizia [2 ]
Molinari, Anna M. [3 ]
Cioffi, Michele [3 ]
Mansi, Luigi [4 ]
Rambaldi, Pierfrancesco [4 ]
DiCioccio, Luigi [5 ]
Cacciapuoti, Federico [1 ]
Canonico, Raffaele [1 ]
Paolisso, Giuseppe [1 ]
机构
[1] Univ Naples 2, Dept Geriatr Med & Metab Dis, Naples, Italy
[2] Italian Natl Res Ctr Aging, Ancona, Italy
[3] Univ Naples 2, Dept Gen Pathol, Naples, Italy
[4] Univ Naples 2, Div Nucl Med, Naples, Italy
[5] Santa Scolastica Hosp, Dept Geriatr Med, Cassino, Italy
关键词
CENTRAL-NERVOUS-SYSTEM; ALZHEIMERS-DISEASE; INSULIN-RESISTANCE; GLUCOSE; MEMORY; RISK;
D O I
10.2337/dc09-2030
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
OBJECTIVE Studies have suggested that insulin resistance plays a role in cognitive impairment in individuals with type 2 diabetes. We aimed to determine whether an improvement in insulin resistance could explain cognitive performance variations over 36 weeks in older individuals with mild cognitive impairment (MCI) and type 2 diabetes. RESEARCH DESIGN AND METHODS A total of 97 older individuals (mean +/- SD age 76 6 years) who had recently (<2 months) started an antidiabetes treatment of metformin (500 mg twice a day) (n = 30) or metformin (500 mg/day)+ rosiglitazone (4 mg/day) (n = 32) or diet (n = 35) volunteered. The neuropsychological test battery consisted of the Mini-Mental State Examination (MMSE), Rey Verbal Auditory Learning Test (RAVLT) total recall, and Trail Making Tests (TMT-A and TMT-B) performed at baseline and every 12 weeks for 36 weeks along with clinical testing. RESULTS At baseline, no significant differences were found between groups in clinical or neuropsychological parameters. Mean SD values in the entire population were as follows: A1C 7.5 +/- 0.5%, fasting plasma glucose (FPG) 8.6 +/- 1.3 mmol/l, fasting plasma insulin (FPI) 148 +/- 74 .pmol/l, MMSE 24.9 +/- 2.4, TMT-A 61.6 +/- 42.0, TMT-B 162.8 +/- 78.7, the difference between TMT-B and TMT-A [DIFFBA] 101.2 +/- 58.1, and RAVLT 24.3 +/- 2.1. At follow-up, ANOVA models tested changes in metabolic control parameters (FPI, FPG, and A1C). Such parameters improved in the metformin and metformin/rosiglitazone groups (P-trend < 0.05 in both groups). ANCOVA repeated models showed that results for the metformin/rosiglitazone group remained stable for all neuropsychological tests, and results for the diet group remained stable for the MMSE and TMT-A and declined for the TMT-B (P-trend = 0.024), executive efficiency (DIFFBA) (P-trend = 0.026), and RAVLT memory test (P-trend = 0.011). Results for the metformin group remained stable for the MMSE and TMTs but declined for the RAVLT (P-trend = 0.011). With use of linear mixed-effects models, the interaction term, FPI X time, correlated with cognitive stability on the RAVLT in the metformin/rosiglitazone group (beta = -1.899; P = 0.009). CONCLUSIONS Rosiglitazone may protect against cognitive decline in older individuals with type 2 diabetes and MCI.
引用
收藏
页码:1706 / 1711
页数:6
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